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Auteur Lu Y

Documents disponibles écrits par cet auteur (24)

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Article

Neuromuscular disorders : NMD, Epub. Clinical, pathological, and genetic characterization in a large Chinese cohort with female dystrophinopathy

Liu C ; Ma J ; Lu Y ; Lu Y ; Mai J ; Bai L ; Wang Y ; Zheng Y ; Yu M ; Zheng Y ; Deng J ; Meng L ; Zhang W ; Wang Z ; Yuan Y ; Xie Z | 19/08/2023

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Article

Frontiers in medicine, 10. Prime editing strategies to mediate exon skipping in DMD gene

Happi Mbakam C ; Roustant J ; Rousseau J ; Yameogo P ; Lu Y ; Bigot A ; Mamchaoui K ; Mouly V ; Lamothe G ; Tremblay JP | 25/05/2023

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Annals of clinical and translational neurology Comparison between mono-tacrolimus and mono-glucocorticoid in the treatment of myasthenia gravis

Fan Z ; Lei L ; Su S ; Zhang S ; Xie N ; Li L ; Lu Y ; Di L ; Wang M ; Xu M ; Shen XM ; Da Y | United States | 20/02/2023

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Article

International immunopharmacology, 115. JAK2 inhibitor ameliorates the progression of experimental autoimmune myasthenia gravis and balances Th17/Treg cells via regulating the JAK2/STAT3-AKT/mTOR signaling pathway

Lu Y ; Ma Q ; Yu L ; Huang H ; Liu X ; Chen P ; Ran H ; Liu W | Netherlands | 02/2023

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Article

Pediatric neurology, 140. Pathogenic PSAT1 Variants and Autosomal Recessive Axonal Charcot-Marie-Tooth Disease With Ichthyosis

Lu Y ; Xing H ; Liu C ; Huang D ; Sun C ; Yu M ; Meng L ; Lv H ; Zhang W ; Wang Z ; Yuan Y ; Xie Z | United States | 24/11/2022

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Article

BMC neurology, 22, 1. The clinical, myopathological, and molecular characteristics of 26 Chinese patients with dysferlinopathy: a high proportion of misdiagnosis and novel variants

Wang N ; Han X ; Hao S ; Han J ; Zhou X ; Sun S ; Tang J ; Lu Y ; Wu H ; Ma S ; Song X ; Ji G | England | 01/11/2022

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Article

Molecular therapy. Nucleic acids, 30. Prime editing optimized RTT permits the correction of the c.8713C>T mutation in DMD gene

Happi Mbakam C ; Rousseau J ; Lu Y ; Bigot A ; Mamchaoui K ; Mouly V ; Tremblay JP | United States | 02/10/2022

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Article

The Journal of molecular diagnostics : JMD Comprehensive Analysis of Spinal Muscular Atrophy: SMN1 Copy Number, Intragenic Mutation, and 2 + 0 Carrier Analysis by Third-Generation Sequencing

Li S ; Han X ; Xu Y ; Chang C ; Gao L ; Li J ; Lu Y ; Mao A ; Wang Y | United States | 31/05/2022

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Article

iScience, 25, 5. Molecular characterization of myotonic dystrophy fibroblast cell lines for use in small molecule screening

Jenquin JR ; O'Brien AP ; Poukalov K ; Lu Y ; Frias JA ; Shorrock HK ; Richardson JI ; Mazdiyasni H ; Yang H ; Huigens RW 3rd ; Boykin D ; Ranum LPW ; Cleary JD ; Wang ET ; Berglund JA | 04/04/2022

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Article

Acta neurologica Belgica Clinical evaluation of efficacy of leflunomide combined with low-dose prednisone for treatment of myasthenia gravis

Huang X ; Qiu L ; Lu Y ; Chen J ; Yang W ; Ou C ; Ran H ; Liu W | Italy | 19/08/2021

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Article

International immunopharmacology, 93. Leflunomide ameliorates experimental autoimmune myasthenia gravis by regulating humoral and cellular immune responses

Huang H ; Ran H ; Liu X ; Yu L ; Qiu L ; Lin Z ; Ou C ; Lu Y ; Yang W ; Liu W | Netherlands | 04/2021

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Article

Orphanet journal of rare diseases, 15, 1. Clinical features and genotypes of Laing distal myopathy in a group of Chinese patients, with in-frame deletions of MYH7 as common mutations

Yu M ; Zhu Y ; Lu Y ; Lv H ; Zhang W ; Yuan Y ; Wang Z | 09/12/2020

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Article

Frontiers in neurology, 11. Expanding the Clinico-Genetic Spectrum of Myofibrillar Myopathy: Experience From a Chinese Neuromuscular Center

Luo YB ; Peng Y ; Lu Y ; Li Q ; Duan H ; Bi F ; Yang H | 15/09/2020

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Article

Neuromuscular disorders : NMD AChR myasthenia gravis switching to MuSK or double antibody positive myasthenia gravis in two children and literature review

Lu Y ; Ran H ; Yang W ; Ma Q ; Qiu L ; Ou C ; Chen P ; Lin Z ; Liu W | England | 2020

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Article

Journal of neurology, 266, 2. Limb girdle muscular dystrophy D3 HNRNPDL related in a Chinese family with distal muscle weakness caused by a mutation in the prion-like domain

Sun Y, Auteur ; Chen H ; Lu Y ; Duo J ; Lei L ; OuYang Y ; Hao Y ; Da Y ; Shen XM | 02/2019

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Article

Journal of the neurological sciences, 379. Mitochondrial tRNA genes are hotspots for mutations in a cohort of patients with exercise intolerance and mitochondrial myopathy

Lu Y, Auteur ; Zhao D ; Yao S ; Wu S ; Hong D ; Wang Q ; Liu J ; Smeitink JAM ; Yuan Y ; Wang Z | 2017

Comment in: Serious assessment of mtDNA variants is a prerequisite to confirm pathogenicity. [J Neurol Sci. 2017]

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Article

The Journal of neuroscience : the official journal of the Society for Neuroscience, 34, 42. LRP4 Is Critical for Neuromuscular Junction Maintenance

Barik A ; Lu Y ; Sathyamurthy A ; Bowman A ; Shen C ; Li L ; Xiong WC ; Mei L | 2014

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Article

PLoS ONE, 7, 6, e39288. A novel autosomal dominant inclusion body myopathy linked to 7q22.1-31.1

Lu Y ; Wang M ; Li X ; Zhang F ; Li Y ; Zhang M ; Da Y ; Yu J ; Jia J | 06/2012

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Article

Journal of neuroimmunology, 251, 1-2. Specific immunotherapy of experimental myasthenia gravis in vitro and in vivo: The Guided Missile strategy

Sun W ; Miagkov A ; Lu Y ; Juon HS ; Drachman DB | 2012

Accès au résumé PubMed / to PubMed abstract Myasthénie auto-immune : une stratégie de « missile téléguidé » pour éliminer uniquement les cellules T spécifiques des récepteurs de l’acétylcholine La myasthénie est une maladie neuromusc[...]

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Human gene therapy, 21, 6. Molecular analysis of vector genome structures after liver transduction by conventional and self-complementary adeno-associated viral serotype vectors in murine and nonhuman primate models

Sun X ; Lu Y ; Bish LT ; Calcedo R ; Wilson JM ; Gao G | 2010

Accès au résumé PubMed / to PubMed abstract

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Article

Human gene therapy, 15, 2. Sustained improvement of muscle function one year after full-length dystrophin gene transfer into mdx mice by a gutted helper-dependent adenoviral vector

Dudley RWR ; Lu Y ; Gilbert R ; Matecki S ; Nalbantoglu J ; Petrof BJ ; Karpati G | 02/2004

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Article

Spine, 24, 23. Biomechanics of increased exposure to lumbar injury caused by cyclic loading: Part 1. Loss of reflexive muscular stabilization

Solomonow M ; Zhou BH ; Baratta RV ; Lu Y ; Harris M | 1999

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Article

Spine, 24, 23. Biomechanics of increased exposure to lumbar injury caused by cyclic loading. Part 2. Recovery of reflexive muscular stability with rest

Gedalia U ; Solomonow M ; Zhou BH ; Baratta RV ; Lu Y ; Harris M | 1999

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Article

Journal of electromyography and kinesiology, 8, 4. Ligamento-muscular protective reflex in the lumbar spine of the feline

Stubbs M ; Harris M ; Solomonow M ; Zhou B ; Lu Y ; Baratta RV | 1998

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Détail de l'auteur

Auteur Lu Y

Documents disponibles écrits par cet auteur (24)

Neuromuscular disorders : NMD, Epub. Clinical, pathological, and genetic characterization in a large Chinese cohort with female dystrophinopathy

Frontiers in medicine, 10. Prime editing strategies to mediate exon skipping in DMD gene

Annals of clinical and translational neurology Comparison between mono-tacrolimus and mono-glucocorticoid in the treatment of myasthenia gravis

International immunopharmacology, 115. JAK2 inhibitor ameliorates the progression of experimental autoimmune myasthenia gravis and balances Th17/Treg cells via regulating the JAK2/STAT3-AKT/mTOR signaling pathway

Pediatric neurology, 140. Pathogenic PSAT1 Variants and Autosomal Recessive Axonal Charcot-Marie-Tooth Disease With Ichthyosis

BMC neurology, 22, 1. The clinical, myopathological, and molecular characteristics of 26 Chinese patients with dysferlinopathy: a high proportion of misdiagnosis and novel variants

Molecular therapy. Nucleic acids, 30. Prime editing optimized RTT permits the correction of the c.8713C>T mutation in DMD gene

The Journal of molecular diagnostics : JMD Comprehensive Analysis of Spinal Muscular Atrophy: SMN1 Copy Number, Intragenic Mutation, and 2 + 0 Carrier Analysis by Third-Generation Sequencing

iScience, 25, 5. Molecular characterization of myotonic dystrophy fibroblast cell lines for use in small molecule screening

Acta neurologica Belgica Clinical evaluation of efficacy of leflunomide combined with low-dose prednisone for treatment of myasthenia gravis

International immunopharmacology, 93. Leflunomide ameliorates experimental autoimmune myasthenia gravis by regulating humoral and cellular immune responses

Orphanet journal of rare diseases, 15, 1. Clinical features and genotypes of Laing distal myopathy in a group of Chinese patients, with in-frame deletions of MYH7 as common mutations

Frontiers in neurology, 11. Expanding the Clinico-Genetic Spectrum of Myofibrillar Myopathy: Experience From a Chinese Neuromuscular Center

Neuromuscular disorders : NMD AChR myasthenia gravis switching to MuSK or double antibody positive myasthenia gravis in two children and literature review

Journal of neurology, 266, 2. Limb girdle muscular dystrophy D3 HNRNPDL related in a Chinese family with distal muscle weakness caused by a mutation in the prion-like domain

Journal of the neurological sciences, 379. Mitochondrial tRNA genes are hotspots for mutations in a cohort of patients with exercise intolerance and mitochondrial myopathy

The Journal of neuroscience : the official journal of the Society for Neuroscience, 34, 42. LRP4 Is Critical for Neuromuscular Junction Maintenance

PLoS ONE, 7, 6, e39288. A novel autosomal dominant inclusion body myopathy linked to 7q22.1-31.1

Journal of neuroimmunology, 251, 1-2. Specific immunotherapy of experimental myasthenia gravis in vitro and in vivo: The Guided Missile strategy

Human gene therapy, 21, 6. Molecular analysis of vector genome structures after liver transduction by conventional and self-complementary adeno-associated viral serotype vectors in murine and nonhuman primate models

Human gene therapy, 15, 2. Sustained improvement of muscle function one year after full-length dystrophin gene transfer into mdx mice by a gutted helper-dependent adenoviral vector

Spine, 24, 23. Biomechanics of increased exposure to lumbar injury caused by cyclic loading: Part 1. Loss of reflexive muscular stabilization

Spine, 24, 23. Biomechanics of increased exposure to lumbar injury caused by cyclic loading. Part 2. Recovery of reflexive muscular stability with rest

Journal of electromyography and kinesiology, 8, 4. Ligamento-muscular protective reflex in the lumbar spine of the feline